Third molar surgery.
Conditions
Interventions
Intervention 1: In the first intervention group, one side of the surgical cavity will be washed with 10 ml of normal saline. After washing and ensuring the cleanliness of the surgical site, suturing w
Sponsors
Islamic Azad University, Khorasgan branch
Eligibility
Sex/Gender
All
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Informed consent Patients requiring lower bilateral third molar surgery Age between 18 and 35 years old
Exclusion criteria
Exclusion criteria: History of systemic diseases History of taking nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, antibiotics, and anticoagulants at least two weeks before surgery History of active infection, cyst, or tumor associated with third molars History of sensitivity to the solutions used Patients who consume alcohol and smoke Pregnant or breastfeeding women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain intensity. Timepoint: Day 1, Day 3, Day 7, and Day 14 after surgery. Method of measurement: Using a numerical pain scale.;Limited mouth opening. Timepoint: Day 1, Day 3, Day 7, and Day 14 after surgery. Method of measurement: Using a digital caliper.;Swelling. Timepoint: Day 1, Day 3, Day 7, and Day 14 after surgery. Method of measurement: Using a standard flexible ruler and clinical examination. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSarina Sadeghi
Islamic Azad University, Khorasgan branch
Outcome results
None listed